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TwinLoop Flex Guide, 12° RM B

by T.A.G Medical Products Agricultural Cooperative Association

TwinLoop Flex Guide, 12° RM B (400104st) is a Class I device made by T.A.G Medical Products Agricultural Cooperative Association, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 10810190015428), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10810190015428 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
TwinLoop Flex Guide, 12° RM
Generic name
Arthroscopic obturator
Model / Ref / Catalog
B, 400104st
Primary DI / UDI-DI
10810190015428
FDA product code
LXH
GMDN term
Arthroscopic obturator
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Arthroscopic obturator

Similar devices in this category

Other devices filed under Arthroscopic obturator.

Other devices from T.A.G Medical Products Agricultural Cooperative Association

See all devices from T.A.G Medical Products Agricultural Cooperative Association →

Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (10, all answered No)